Braddock syndrome

Braddock syndrome is a rare malformation syndrome with multiple congenital abnormalities, described in 2 siblings, that is characterized by VACTERL -like association in combination with pulmonary hypertension, laryngeal webs, blue sclerae, abnormal ears, persistent growth deficiency and normal intellect.

Also known as: Vater-like syndrome with pulmonary hypertension, abnormal ears and growth deficiency, VATER-like defects with pulmonary hypertension, laryngeal webs, and growth deficiency

21 clinical trials for this condition and its sub-types, 0 tagged with Braddock syndrome itself.